Rearrangement of 2,2-disubstituted cyclohexane-1,3-diones in polyphosphoric acid
β Scribed by A.M. Chalmers; A.J. Baker
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 201 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Current interest"3 in the Robinson-Mannich annelation of cyclohexane-l,j-dione prompts us to report an aspect of acid catalyeed reactions of 2,2-disubetituted cyolohexane-l,Jdiones using polyphoephoric acid4.
π SIMILAR VOLUMES
The isomerisation of 1,4-diarvl-2-azetidinones in cold concentrated sulohuric acid to qive the correspondinq 3,4-dihydro-4-arylquinolin-2(1H)-ones (e.a. la + 2a) was first reported hy Knunyants and Gambaryan' and the results were recently confirmed and extended2. We have found that the chloro-comnou
## Abstract The title condensations gave respectively: __gem__βbisarylated cyclic amines **3aβk** or monoarylated unsaturated cyclic amines **4aβg**, 1,3βbisarylated cyclohexadienes **6a**, **6b**, the condensed bicyclo [2,2,2]βoctane **8**. In addition the aromatic ketone **9** gave the fluorenone